Abstract:There is a need to develop inexpensive, portable and easy-to-use devices for viral sample processing for resource-limited settings. Here we offer a solution to efficient virus capture by incorporating macroporous materials with regular structures into microfluidic devices for affinity chromatography. Two-dimensional simulations were first conducted to investigate the effects of two structures, a nanopost array and a spherical pore network, on nanoparticle capture. Then, the two structures were created in polym… Show more
“…352 Nanostructures have more binding sites than planar surface, enabling viral particle enrichment and signal amplification. 230,353 Yu et al, for example, developed a microdevice incorporating ZnO nanorods to enrich and identify avian influenza virus. 354 With the assistance of threedimensional nanorods, this method achieved a detection limit of 3.6 × 103 EID 50 mL −1 , which is ∼22 times more sensitive than a conventional ELISA assay.…”
Section: Conclusion and Future Perspectivesmentioning
“…352 Nanostructures have more binding sites than planar surface, enabling viral particle enrichment and signal amplification. 230,353 Yu et al, for example, developed a microdevice incorporating ZnO nanorods to enrich and identify avian influenza virus. 354 With the assistance of threedimensional nanorods, this method achieved a detection limit of 3.6 × 103 EID 50 mL −1 , which is ∼22 times more sensitive than a conventional ELISA assay.…”
Section: Conclusion and Future Perspectivesmentioning
“…In recent years, virus sample preparation has also attracted more attention and there have been different proposals for viral sample preparation strategies. For different detection methods, sample preparation have different meanings such as sample enrichment (Surawathanawises et al, 2016) or nucleic acid extraction (Chen et al, 2019;. Recently, Du et al (Du et al, 2017a) proposed an automated sample preparation microfluidic system that utilized air bubbles and magnetic beads to achieve efficient capture of the Ebola virus.…”
“…However, better LOD can be reached by complexifying the microdevices while keeping the sample processing as a simple flow-through process. For instance, enhancement of viral detection is obtained by the fabrication of porous devices with a nanopore array over flatbed microchannels [85]. The system was tested with biotinylated HIV virions captured in channels with surface functionalized with Avidin (NeutrAvidin).…”
Section: Microfluidic Applications In Hiv-1 Basic Researchmentioning
confidence: 99%
“…The system was tested with biotinylated HIV virions captured in channels with surface functionalized with Avidin (NeutrAvidin). High HIV capture yields (80%) are reached for a large range of HIV concentrations (10 3 -10 6 virions/mL) [85]. A clever biosensing system has also been proposed that consists in electrical sensing viruses through capacitance spectroscopy on a flexible plastic chip with printed electrodes.…”
Section: Microfluidic Applications In Hiv-1 Basic Researchmentioning
HIV-1 is the causative agent of acquired immunodeficiency syndrome (AIDS). It affects millions of people worldwide and the pandemic persists despite the implementation of highly active antiretroviral therapy. A wide spectrum of techniques has been implemented in order to diagnose and monitor AIDS progression over the years. Besides the conventional approaches, microfluidics has provided useful methods for monitoring HIV-1 infection. In this review, we introduce continuous microfluidics as well as the fabrication and handling of microfluidic chips. We provide a review of the different applications of continuous microfluidics in AIDS diagnosis and progression and in the basic study of the HIV-1 life cycle.
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